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51220-50-9

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51220-50-9 Usage

Description

DL-Norvaline methyl ester is a chemical compound derived from the amino acid norvaline, characterized by its methyl ester functional group. It is primarily utilized in research settings to investigate its effects on biological systems.

Uses

Used in Pharmaceutical Research:
DL-Norvaline methyl ester is used as a research compound for exploring its potential antioxidant and anti-inflammatory properties. Its application in this field is driven by the need to understand its effects on the body and its potential to contribute to the development of new drugs.
Used in Drug Development:
In the pharmaceutical industry, DL-Norvaline methyl ester is used as a precursor in the synthesis of new drugs. Its potential applications include the development of treatments for cardiovascular disease and cancer, although further research is necessary to fully comprehend its benefits and any possible side effects.
Overall, DL-Norvaline methyl ester is a promising compound with potential applications in medicine and health, warranting continued research to unlock its full potential.

Check Digit Verification of cas no

The CAS Registry Mumber 51220-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,2 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51220-50:
(7*5)+(6*1)+(5*2)+(4*2)+(3*0)+(2*5)+(1*0)=69
69 % 10 = 9
So 51220-50-9 is a valid CAS Registry Number.

51220-50-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (3R)-aminopentanoate

1.2 Other means of identification

Product number -
Other names norvaline methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51220-50-9 SDS

51220-50-9Relevant articles and documents

TRIAZOLE DERIVATIVE

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Page/Page column 21-22, (2008/06/13)

A compound represented by the formula (I) below or a pharmaceutically acceptable salt thereof has an effect of inhibiting binding between S1P and its receptor Edg-1(S1P1), and is useful as a pharmaceutical product. (I) (In the formula, A represents a sulfur atom, an oxygen atom, a formula -SO- or a formula -SO2-; R1 represents a hydrogen atom, an alkyl group having 1-6 carbon atoms or the like; R2 represents an alkyl group having 1-6 carbon atoms, a cycloalkyl group having 3-8 carbon atoms or the like; R3 represents a hydrogen atom or an alkyl group having 1-6 carbon atoms; R4 represents a hydrogen atom, an alkyl group having 1-6 carbon atoms, a phenyl group or the like; R5 represents a hydrogen atom or an alkyl group having 1-6 carbon atoms; and R6 represents an alkyl group having 1-6 carbon atoms, a phenyl group or a substituted phenyl group.)

A Facile Synthesis of α-Amino Esters via Reduction of α-Nitro Esters Using Ammonium Formate as a Catalytic Hydrogen Transfer Agent

Ram, Siya,Ehrenkaufer, Richard E.

, p. 133 - 135 (2007/10/02)

Various nitroesters 3 were selectively and rapidly reduced to their corresponding amino esters 4 in very good yield using anhydrous ammonium formate as a catalytic hydrogen transfer agent.

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